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Translation of "Déficience intellectuelle liée à l'X type Nascimento " (French → English) :
TERMINOLOGY
see also In-Context Translations below déficience intellectuelle liée à l'X type Nascimento
X-linked intellectual disability, nail dystrophy, seizures syndrome
SNOMEDCT-BE (disorder) / 726732002
SNOMEDCT-BE (disorder) / 726732002
déficience intellectuelle liée à l'X type Stocco Dos Santos
This syndrome is characterized by severe intellectual deficit with hyperactivity, language delay, congenital hip luxation, short stature, kyphosis and recurrent respiratory infections. Aggressive behavior and frequent epileptic seizures may also be p
SNOMEDCT-BE (disorder) / 718910006
SNOMEDCT-BE (disorder) / 718910006
déficience intellectuelle liée à l'X type Cantagrel
Characterized by marked neonatal hypotonia, progressive quadriparesis, severely delayed developmental milestones (walking at 3 years of age), gastroesophageal reflux, and stereotypic movements of the hands, esotropia and infantile autism. It has been
SNOMEDCT-BE (disorder) / 719016007
SNOMEDCT-BE (walking at 3 years of age), gastroesophageal reflux, and stereotypic movements of the hands, esotropia and infantile autism. It has been / 719016007
déficience intellectuelle liée à l'X type Snyder
Snyder-Robinson syndrome
SNOMEDCT-BE (disorder) / 702416008
SNOMEDCT-BE (disorder) / 702416008
déficience intellectuelle liée à l'X type Turner
X-linked mental retardation, Turner type has characteristics of moderate to severe intellectual deficit in boys and moderate intellectual deficit in girls. It has been described in 14 members from four generations of one family. Macrocephaly was repo
SNOMEDCT-BE (disorder) / 718912003
SNOMEDCT-BE (disorder) / 718912003
déficience intellectuelle liée à l'X type Pai
This syndrome has characteristics of the association of dysmorphism with intellectual deficit. It has been described in four generations of one family. Premature death was reported in the affected males. Transmission is X-linked recessive and the cau
SNOMEDCT-BE (disorder) / 719011002
SNOMEDCT-BE (disorder) / 719011002
déficience intellectuelle liée à l'X type Cabezas
Cabezas syndrome
SNOMEDCT-BE (disorder) / 719811001
SNOMEDCT-BE (disorder) / 719811001
déficience intellectuelle liée à l'X type Cilliers
X-linked intellectual disability Cilliers type
SNOMEDCT-BE (disorder) / 719013004
SNOMEDCT-BE (disorder) / 719013004
déficience intellectuelle liée à l'X type Abidi
This syndrome has characteristics of X-linked intellectual deficit and mild variable manifestations, including short stature, small head circumference, sloping forehead, hearing loss, abnormally shaped ears, and small testes. It has been described in
SNOMEDCT-BE (disorder) / 719018008
SNOMEDCT-BE (disorder) / 719018008
déficience intellectuelle liée à l'X type Armfield
Armfield syndrome
SNOMEDCT-BE (disorder) / 719017003
SNOMEDCT-BE (disorder) / 719017003
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Déficience intellectuelle liée à l'X type Nascimento
Date index:2022-02-14 -
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